Taiwan FDA registration 5160fa1f968cc1c1352a5063f5443884

"Minjian" neti wash (unsterilized)

TW: "民健"洗鼻器 (未滅菌)

Taiwan·Risk Class 1·JIANN GWO PLASTIC INDUSTRY CO., LTD.·Registered Aug 24, 2015 – Aug 24, 2025Expired

Registration details

Analysis ID: 5160fa1f968cc1c1352a5063f5443884

Company information

Manufacturer: JIANN GWO PLASTIC INDUSTRY CO., LTD.
Manufacturer Country: Taiwan, Province of China
Authorized Representative: MIN CHIEN INDUSTRIAL CO., LTD.

Product details

Intended Use: Limited to the first level of identification scope of the Measures for the Classification and Grading of Medical Devices "ENT Dispensing Devices and Substances Used Together (G.5220)".
Product Type (Level 1): G ENT Science
Product Type (Level 2): G.5220 Ear, nose and throat applicators and substances used in conjunction thereof
Import Information: Contract manufacturing;; Domestic

Dates and status

Registration Date: Aug 24, 2015
Expiry Date: Aug 24, 2025

About this record

Access comprehensive regulatory information for "Minjian" neti wash (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 5160fa1f968cc1c1352a5063f5443884 and manufactured by JIANN GWO PLASTIC INDUSTRY CO., LTD.. The authorized representative in Taiwan is MIN CHIEN INDUSTRIAL CO., LTD..

This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.